Canonical Allele Identifier: CA1525635728

Gene: ADCY2

Linked Data

• dbSNP Id: rs1744290938
• gnomAD v3: 5-7517370-C-CTT
• gnomAD v4: 5-7517370-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7517374_7517375dup , CM000667.2:g.7517374_7517375dup	GRCh38
NC_000005.9:g.7517487_7517488dup , CM000667.1:g.7517487_7517488dup	GRCh37
NC_000005.8:g.7570487_7570488dup	NCBI36
NG_046913.1:g.126145_126146dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000338316.9:c.409-3364_409-3363dup MANE Select	ENSP00000342952.4:n.409-3364_409-3363dup
ENST00000338316.8:c.409-3364_409-3363dup	ENSP00000342952.4:n.409-3364_409-3363dup
ENST00000484965.5:n.143-3364_143-3363dup
ENST00000498598.1:n.108-3364_108-3363dup
ENST00000537121.5:c.409-3364_409-3363dup	ENSP00000444803.2:n.409-3364_409-3363dup
NM_020546.2:c.409-3364_409-3363dup	NP_065433.2:n.409-3364_409-3363dup
XM_011513942.1:c.409-3364_409-3363dup	XP_011512244.1:n.409-3364_409-3363dup
XR_427657.2:n.423-3364_423-3363dup
XM_011513942.2:c.409-3364_409-3363dup	XP_011512244.1:n.409-3364_409-3363dup
XR_001741973.1:n.423-3364_423-3363dup
XR_001741974.2:n.423-3364_423-3363dup
NM_020546.3:c.409-3364_409-3363dup MANE Select	NP_065433.2:n.409-3364_409-3363dup